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A de novo heterozygous point mutation in the p63 gene causing the syndrome of ectrodactyly, ectodermal dysplasia and facial clefting

✍ Scribed by G. Pozo; S. Canún; S. Kofman-Alfaro; J.C. Zenteno

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

EEC (Ectrodactyly, Ectodermal dysplasia,

✍ A.P. South; G.H.S. Ashton; C. Willoughby; I.H. Ellis; O. Bleck; T. Hamada; G. Ma 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 143 KB

De novo missense mutation, S541Y, in the

✍ V. Shotelersuk; S. Janklat; P. Siriwan; S. Tongkobpetch 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 231 KB

A Novel Heterozygous Point Mutation in t

✍ Miguel Cabanillas; Antonio Torrelo; Benigno Monteagudo; Oscar Suárez-Amor; Aquil 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 227 KB

A Case of Ankyloblepharon, Ectodermal Dy

✍ Yvonne E. Chiu; Beth A. Drolet; Kelly J. Duffy; Kristen E. Holland 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 232 KB

Molecular basis of EEC (ectrodactyly, ec

✍ S.E. Clements; T. Techanukul; D. Coman; J.E. Mellerio; J.A. McGrath 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 467 KB